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FDA 510(k)

RAPID-FOAM

K-Number: K952457 · 1995-08-23

ApplicantThe Soule Co., Inc.
Decision Date1995-08-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RAPID-FOAM is the device name listed in this FDA 510(k) record. The listed applicant is The Soule Co., Inc.. It received FDA 510(k) clearance on 1995-08-23 under 510(k) number K952457. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAPID-FOAM?

RAPID-FOAM is a medical device that received FDA 510(k) clearance on 1995-08-23. The listed applicant is The Soule Co., Inc.. The 510(k) number is K952457.

When did RAPID-FOAM receive FDA 510(k) clearance?

RAPID-FOAM received FDA 510(k) clearance on 1995-08-23, under 510(k) number K952457.

Who is the listed applicant for RAPID-FOAM?

The FDA 510(k) record lists The Soule Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAPID-FOAM?

The FDA product code for RAPID-FOAM is IYE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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